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Recipharm Stockhom AB Form 483 Details

Form 483
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Source: FDA inspection recordConfirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months.

To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3003741149.

Recipharm Stockhom AB

Stockholm, -, Sweden
Issue DateSeptember 13, 2011
FEI Number3003741149
CountrySweden
Status
No Warning Letter
Product Type
Drugs
Recipharm Stockhom AB FDA Form 483, Stockholm, September 13, 2011